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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)

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Cole, P.D. et al.

Cole, Kamen,

Delayed neurotoxicity associated with therapy for children with acute lymphoblastic leukemia.

Most children diagnosed today with acute lymphoblastic leukemia (ALL) will be cured. However, treatment entails risk of neurotoxicity, causing deficits in neurocognitive function that can persist in the years after treatment is completed. Many of the components of leukemia therapy can contribute to adverse neurologic sequelae, including craniospinal irradiation, nucleoside analogs, corticosteroids, and antifolates. In this review, we describe the characteristic radiographic findings and neurocognitivie deficits seen among survivors of childhood ALL. We summarize what is known about the pathophysiology of delayed treatment-related neurotoxicity, with a focus on the toxicity resulting from pharmacologic disruption of folate physiology within the central nervous system. Finally, we suggest testable strategies to ameliorate the symptoms of treatment-related neurotoxicity or decrease its incidence. MRDD Research Reviews 2006;12:174-183. (c) 2006 Wiley-Liss, Inc.[1]

References

Delayed neurotoxicity associated with therapy for children with acute lymphoblastic leukemia. Cole, P.D., Kamen, B.A. Mental retardation and developmental disabilities research reviews. (2006) [Pubmed]

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